Aunt Minnies Pulmo Flashcards

1
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Swyer–James Syndrome

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2
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Surfactant Deficiency Disease.

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3
Q
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Meconium Aspiration.

-Hyperinflation and coarse linear and nodular opacities throughout both lungs is typical of meconium aspiration.

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4
Q
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Retained Lung Fluid.

-Linear opacities, central greater than peripheral particularly when radiating from the hila
-resolves within 72h of life

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5
Q
A

Bilateral Pneumothoraces in a Neonate.

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6
Q
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Skin Fold

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7
Q
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Pneumomediastinum

“ Angel wing” sign (*)

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8
Q
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Umbilical venous catheter (arrowhead) enters at the umbilicus and extends cephalad, while the umbilical arterial catheter (arrow) extends caudal and then makes an acute angle and extends cephalad.

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9
Q
A

Extracorporeal Membrane Oxygenation (ECMO)

The venous catheter (1) atrium. Enters IJV to RA
The arterial catheter (2) enters the common carotid artery and ends just above the aortic arch.

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10
Q
A

Congenital Pulmonary Airway Malformation

Type I: MC; >2cm

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11
Q
A

Mediastinal Bronchogenic Cyst

-round, well-defined masses that can occur in mediastinum or in the lung, usually centrally
-air within one suggests infection

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12
Q
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Scimitar or Hypogenetic Lung Syndrome.

-abnormal drainage of a lobe to the IVC, hepatic vein, or left atrium.

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13
Q
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Round Pneumonia

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14
Q
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Croup

“steeple or pencil point sign.”
-epiglottis (*) is normal; aryepiglottic folds (arrowhead) which should be thin.

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15
Q
A

Bacterial Tracheitis

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16
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Bacterial Tracheitis

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17
Q
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Epiglottitis.

The epiglottis (arrow) is broad and short. The aryepiglottic folds are thickened (*)

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18
Q
A

Pancoast (superior sulcus) tumor

  • majority of these lesions are squamous cell carcinomas or adenocarcinoma
19
Q
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Pleural Lipoma
-MC focal pleural mass

20
Q
A

Pleural Lipoma
-MC focal pleural mass

21
Q
A

Holly Leaf appearance (Asbestos inhalation)

22
Q
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Flail chest

23
Q
A

Pectus Excavatum

*Autosomal Dominant

24
Q
A

Pectus carinatum

25
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Diaphragmatic Eventration

26
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Traumatic Diaphragmatic Hernia

27
Q
A

Morgagni hernia

28
Q
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Bochdalek hernia

29
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Honeycomb cysts

  • posterior subpleural regions of both lower lobes,
  • Seen in: UIP, chronic hypersensitivity pneumonitis, sarcoidosis
30
Q
A

Langerhans cell histiocytosis of lung (LCH)

31
Q
A

Lymphangioleiomyomatosis (LAM)

32
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33
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34
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UIP (Usual Interstitial Pneumonia)

35
Q
A

Reversed halo sign

  • cryptogenic organizing pneumonia
36
Q
A

Tracheobronchomegaly “Mounier-Kuhn syndrome”

37
Q
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Tracheobronchomalacia

  • crescentic frown-like configuration of the trachea (hallmark)
38
Q
A

Broncholithiasis

39
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Bullous lung disease

40
Q
A
Left Lower Lobe Collapse
41
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A

Right upper lobe collapse

42
Q
A

Phrenic Nerve Palsy

43
Q
A

Left upper lobe collapse

44
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A